
Quinones and Derivatives
Quinones are aromatic compounds containing a benzene ring system with two carbonyl groups in specific positions, forming a cyclohexene structure with oxygen. They are derived from compounds such as anthraquinone and 1,4-benzoquinone, which play important biological roles, including electron transfer in metabolic processes. Quinone derivatives, such as hydroquinones and antirheumatic agents, have applications in the pharmaceutical industry due to their antioxidant, antimicrobial, and anticancer properties. Additionally, quinones are used in the production of dyes and cosmetic products.
At CymitQuimica, we offer quinones and their derivatives for applications in organic chemistry, pharmaceuticals, and the cosmetic industry.
Found 24182 products of "Quinones and Derivatives"
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
3-[6-Chloro-4-(trifluoromethyl)pyridin-2-yl]benzoic acid
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:301.6499938964844Alternariol
CAS:<p>Stability Hygroscopic<br>Applications Alternariol is an alternaria mycotoxin and genotoxin, found in common edible crops. It inhibits the activity of various DNA-topoisomerases, increasing the rate of DNA strand breaks.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Asam S et al. J Agric Food Chem. 2009 Jun 24;57(12):5152-60.Fehr M et al. Mol Nutr Food Res. 2009 Apr;53(4):441-51Vejdovszky K. et al. Toxicol Lett. 2017 Feb 5;267:45-52.<br></p>Formula:C14H10O5Color and Shape:Light BrownMolecular weight:258.23Sterigmatocystin
CAS:<p>Applications Sterigmatocystin is a carcinogenic mycotoxin that is struturally related to Aflatoxin. Sterigmatocystin has been shown to inhibit RNA synthesis in rat liver nuclei.Environmental contaminants; Food contaminants<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Nel, W. et al.: Biochem. Pharmacol., 19, 957 (1970); Purchase, I.F.H. et al.: Food Cosm. Toxicol., 8, 289 (1970);<br></p>Formula:C18H12O6Color and Shape:Light YellowMolecular weight:324.283,3'-dinitrobiphenyl-4,4'-diamine
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:274.23599243164065-Biphenyl-4-yl-1H-pyrazole-3-carboxylic acid methyl ester
Purity:95.0%Molecular weight:278.3110046386719Podophyllotoxin 4-O-Glucoside
CAS:Controlled Product<p>Applications Podophyllotoxin 4-O-glucoside is the glucoside derivative of Podophyllotoxin (P681000), a skin treatment for genital warts caused by some types of HPVs.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Marques, J.V., et al.: J. Biol. Chem., 288, 466 (2013); Kelly, M.G. & Hartwell, J.L.; J. of the Nat'l Cancer Inst., 14, 967 (1954); Gupta, R.S.; Somatic Cell Genetics, 7, 59 (1981); Gupta, R.S.; Cancer Research, 43, 505 (1983)<br></p>Formula:C35H36O13Color and Shape:NeatMolecular weight:664.65Patulin
CAS:<p>Stability Hygroscopic<br>Applications Patulin (PAT), a mycotoxin produced by certain species of Penicillium, Aspergillus, and Byssochlamys, is mainly found in ripe apple and apple products. Patulin-induced genotoxicity and modulation of glutathione in Hep G2 cells. Patulin is an antibiotic. Patulin-induced nephropathy and gastrointestinal tract malfunction have been demonstrated in several animal models. The oral LD50 value of patulin ranges between 29 and 55 mg/kg body weight in rodents and 170 mg/kg body weight in poultry. The World Health Organization considers patulin cytotoxic and established a safety level of patulin in apple juice at 50 μM. At 100-200 μM, patulin can directly increase intracellular oxidative stress in HEK293 and HL-60 cells. In 1944, this compound was tested in a clinical trial for potential antibiotic<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Scott, P., et al.: J. Agric. Food Chem., 20, 450 (1972), Aden, D., et al.: Nature, 282, 615 (1979), Surralles, J., et al.: Mutat. Res., 341, 169 (1995), Alves, I., et al.: Mutagenesis, 15, 229 (2000), Liu, B., et al.: Toxicol. Appl. Pharmacol., 191, 255 (2003), Puel, O., Galtier, P., and Oswald, I.P. Biosynthesis and toxicological effects of patulin. Toxins 2(4) 613-631 (2010). Liu, B., Wu, T., Yu, F., et al. Induction of oxidative stress response by the mycotoxin patulin in mammalian cells. Toxicol Sci 95(2) 340-347 (2007). Chalmers, I., and Clarke, M. Commentary: The 1994 patulin trial: The first properly controlled multicentre trial conducted under the aegis of the British Medical Research Council. Int J Epidemiol 32 253-260 (2004).<br></p>Formula:C7H6O4Color and Shape:Off-White To YellowMolecular weight:154.12

